Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description

Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
We are seeking a highly skilled DM/Safety Review/Medical Review/Central Monitoring Programmer with expertise in TIBCO Spotfire and JReview (J-Review), along with solid clinical domain knowledge, to design, develop, and support interactive dashboards for clinical data review and safety monitoring. The role involves close collaboration with cross-functional teams to deliver high-quality, compliant, and insight-driven visualizations for clinical decision-making.

Key Responsibilities
Design, develop, and maintain complex Spotfire, JReview, allied analytics tool dashboards for clinical data review
Perform data wrangling and transformation using Spotfire Data Canvas/Jreview/Python etc.




Implement data-on-demand solutions and optimize dashboard performance for large datasets
Translate clinical and business requirements into intuitive analytical dashboards
Develop automated QC visualizations and standardized reporting solutions for global clinical trials
Create and manage information models, data connections, information links, and data functions
Utilize IronPython, HTML, and scripting to enhance dashboard functionality
Support users in creating and modifying dashboards and integrating data from multiple sources
Perform troubleshooting, debugging, and performance tuning of Spotfire applications
Ensure compliance with clinical data standards (SDTM) and regulatory requirements
Collaborate with stakeholders to define timelines, deliverables, and project expectations
JReview (J-Review) for clinical data review and visualization
Must have understanding or hands on experience of Clinical domain, drug development process (Phase I

📌 Cdm Programmer Ii Bengaluru
🏢 Thermo Fisher Scientific
📍 Bengaluru